From: Steve on
Public release date: 7-Aug-2008

Contact: Lorinda Klein/Jennifer Berman
NYU Langone Medical Center / New York University School of Medicine

NYU researchers demonstrate activity of mebendazole in metastatic melanoma

Novel assay finds that widely prescribed anti-parasite drug targets
cancer-causing protein

NEW YORK, August 6, 2008 - Researchers at the NYU Cancer Institute and the
Ronald O. Perelman Department of Dermatology have identified mebendazole, a
drug used globally to treat parasitic infections, as a novel investigational
agent for the treatment of chemotherapy-resistant malignant melanoma.

Because most patients with metastatic melanoma fail to respond to available
therapies, the discovery of a viable investigational treatment with an
established safety profile could address a serious unmet need in oncology.
Effectively sidestepping the prohibitive costs and long lead times typically
required to discover new cancer medicines, the NYU team screened a library
of already approved drugs for activity against the most deadly form of skin
cancer.

Their report, which was selected for advance online publication by Molecular
Cancer Research, is published in the August issue of the journal. Since
submitting the article for publication, the authors have conducted
additional pre-clinical studies of mebendazole in an in vivo model of
chemotherapy-resistant melanoma and are now preparing a phase I clinical
trial, expected to begin next year at NYU Cancer Institute.

"While rational drug design remains a perfectly valid way to develop cancer
therapies, we also need approaches that are less costly and more productive
of new effective treatments," said lead author Seth J. Orlow, M.D. Ph.D.,
Chair of the Ronald O. Perelman Department of Dermatology at New York
University School of Medicine. "You could say this is more of a guerrilla
approach. Instead of screening millions of untested compounds for an agent
that inhibits or stimulates a particular molecular target, we chose to
screen a large library of already approved drugs for novel activity against
melanoma cells, and then advance the most promising candidate rapidly to
clinical practice."

First, the NYU researchers screened a library of 2,000 well-known drugs
[Spectrum Collection (Microsource Discovery Systems)] and identified members
of the benzimidazole family for their ability to inhibit melanoma growth and
induce programmed cell death (apoptosis) of malignant melanoma cells without
affecting normal melanocytes (pigment-producing cells). Of the identified
benzimidazoles, the team selected mebendazole for further study because it
was known to be a well-tolerated, orally available drug with anti-cancer
properties.

In a surprising discovery, the team found that mebendazole takes advantage
of a special difference between a melanoma cell and normal melanocytes.
Melanomas produce high levels of a protein called Bcl-2, which is known to
protect certain cancer cells from apoptosis. The team saw that when a
melanoma cancer cell was exposed to mebendazole, it resulted in inactivation
of Bcl-2, allowing apoptosis to occur.

Mebendazole, sold as a generic drug in the United States, has been used
since the 1970s to treat roundworm, hookworm, pinworm, whipworm, and other
worm-based parasitic infections. Previous research has shown it to have some
antitumor activity in lung and adrenocortical cancer.

"Our ability to identify novel treatments for melanoma and advance them
rapidly into the clinic very much depends on NYU's multidisciplinary
approach to melanoma care and research," Dr. Orlow said. "To be effective,
translational medicine cannot be unidirectional. Discovery moves
continuously back and forth between the clinic and the bench. We are now
focused on determining the range of doses to be tested in the clinic,
whether specific types of melanomas will respond better than others, and
whether combining mebendazole with other agents will be of further benefit"


###
The authors of this study are NYU Cancer Institute researchers Nicole
Doudican, Adrianna Rodriguez, Iman Osman, and Seth J. Orlow. The study was
supported by private philanthropic grants.

..


From: Dan Mayolo on
If one was to try treatment with mebendazole, what would be the
prescription?
What dosage and for how much time?
From: J on
Dan Mayolo wrote:

> If one was to try treatment with mebendazole, what would be the
> prescription?
> What dosage and for how much time?

Phase I trial is next year.
That's when protocols and doses are decided.
J